510(k) K960518 ยท BZD Ventilator, Non-Continuous (Respirator)
THE PURITAN-BENNETT 318 PLUS NASAL CPAP SYSTEM
| Applicant | Puritan Bennett Corp., Lenexa KS, US |
| Decision | Substantially Equivalent, May 9, 1996 |
| Received | Feb 5, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960518
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.